Preparation of 21-deoxy steroids



United States Patent 3,440,252 PREPARATION OF 21-DEOXY STEROIDS Niall Galbraith Weir, Wembley, Middlesex, England, as-

signor to Glaxo Laboratories Limited, Greenford, Middlesex, England, a British company No Drawing. Filed June 21, 1966, Ser. No. 559,083 Int. Cl. C07c 167/00, 169/36 US. Cl. 260397.45 18 Claims ABSTRACT OF THE DISCLOSURE 17oz acyloxy 20 keto-Zl-su'bstituted steroids of the pregnane series are converted to l7a-acyloxy-20-keto-2lunsubstituted steroids by heating with a tertiary amine or dialkyl sulfoxide when the 21-substituent is iodine and, if such heating is conducted in the presence of a metal iodide, also when the 21-substituent is bromine or hydrocarbonsulfonyloxy.

This invention is concerned with a process for the production of 17-tz-monoesters of l7-a-hydroxy-20-ketosteroids of the pregnane series.

Various 17ot-monoesters of 17u-hydroxy-20-keto compounds of the pregnane series have useful anti inflammatory action, especially valuable examples of such compounds being described in our application S.N. 466,434, filed June 23, 1965, now Patent No. 3,376,193. Compounds having anti-inflammatory action will have as is well known, certain substituents in the nucleus, necessary for activity, namely a keto group at the 3-position, a double bond at the 4-position or 1- and 4-positions and either an oxygen function e.g. a hydroxy group at the 11 ,H-position or chlorine at both the 9aand 11 fi-positions. Additional substituents enhancing or modifying activity may also be present e.g. a fluorine atom at the 9-position and/or fluorine atoms, methyl and hydroxyl groups etc. e.g. at the 2,6- or 16-positions.

An object of the present invention is to provide a convenient method for the preparation of 17u-monoesters of 17a-hydroxy-20-keto compounds of the pregnane series, particularly compounds having anti infiammatory action or precursors or intermediates therefor. It is a particular object of the invention to provide a convenient method of producing such 17a-monoesters of compounds having an additional hydroxy group in the nucleus e.g. at the 11- position. Thus attempts to acylate an 1lfi,17a-dihydroxy 20-keto-pregnane compound at the 170t-POSltIOI1 are generally not entirely successful and additional acylation at position 11 frequently occurs.

17u-monoesters of 17a,21-dihydroxy 20-keto steroids can be prepared in comparatively simple manner by first converting the 17a,21-dihydroxy compound to a 17a,21- orthoester which may then be hydrolysed with acid to the 17a-monoester (see US. Patent No. 3,152,154). This method of preparation in general gives rise to little risk of acylation of any hydroxy group which may be present at the 11,8-position.

The present invention provides a process for the preparation of a 17a acyloxy steroid of the pregnane series having at position 17 the formula:

which comprises heating a 21-iodo-17a-acyloxy steroid of the pregnane series having at position 17 the formula:

17 (III) where R in Formulae II and III is an alkyl, cycloalkyl, cycloalkylalkyl or aralkyl group, with a tertiary amine or dialkyl sulphoxide.

In a modification of the process according to the invention a pregnane compound having at position 17 the formula:

---OCOR 17 where X is a hydrocarbon sulphonyloxy radical or a bromine atom and R is an alkyl, cycloalkyl, cycloalkylalkyl or aralkyl group, is heated with a metal iodide e.g. an alkali metal or alkaline earth metal iodide in the presence of a tertiary amine or a dialkyl sulphoxide.

While we do not wish to be limited by theoretical explanations we believe that the modified process proceeds by intermediate formation of the 21-iodo compound.

The group R is preferably a lower alkyl group having from 1 to 7 or more carbon atoms.

The cycloalkyl groups preferably contain 5 or 6 carbon atoms and the cycloalkylalkyl group is preferably a cycloalkylmethyl group.

Examples of tertiary amines which can be used include pyridine, collidine, dimethylaniline and triloweralkylamines e.g. triethylamine or tripropylamine. Examples of dialkyl sulphoxides include the lower alkyl sulphoxides such as dimethyl sulphoxide.

The above reactions may be carried out as necessary in the presence of an additional inert solvent and preferred inert solvents include ketones e.g. acetone and methylethyl ketone, alkanols e.g. ethanol, methanol and isopropanol, and substituted amide solvents e.g. dimethyl formamide.

The hydrocarbon radical of the sulphonyl group may be any convenient alkyl, aryl or alkaryl group e.g. a lower alkyl 'or loweralkylaryl group especially those where the alkyl moieties contain from 1 to 6 carbon atoms. e.g. methyl or p-tolyl etc.

The conversion of Compound I to Compound II or of Compound III to Compound II is preferably effected by heating at temperatures of from 60 C. to 120 C., if necessary under pressure where the boiling point of the tertiary amine, sulphoxide or solvent is below that of the selected reaction temperature. A convenient reaction temperature is C. or alternatively the boiling point of the tertiary amint, dialkyl sulphoxide or solvent if this is below 100 C.

21-bromo compounds of Formula I may for example, be prepared by reacting the corresponding 21-hydrocarbon sulphonyloxy compounds with an alkali metal or alkaline earth metal bromide such as sodium, lithium or calcium bromide under anhydrous conditions in a solvent e.g. acetone, ethanol, acetonitrile, or dimethyl formamide. This reaction is preferably effected at temperatures of from 50 C. to C., conveniently at the boiling point of the solvent used. Relatively long reaction times are generally necessary which may amount to several days.

The 21-iodo compounds of Formula III may be formed either directly from tthe corresponding 21-hydrocarbon sulphonyloxy compounds or from the corresponding 21-bromo compounds the latter method being preferred to the former. The direct formation of the 21-iodo compound either from the hydrocarbon sulphonyloxy compound, or from the 21-bromo compound is effected by heating with an alkali metal or alkaline earth metal iodide in the presence of a solvent such as acetone, ethanol, acetonitrile or dimethyl formamide, The reaction is preferably carried out at temperatures of from 50 C. to 120 C. conveniently at the boiling point of the solvent used. The conversion of the 21-sulphonyloxy compounds to the 21-iodo compounds is slow, being frequently incomplete even after 8 days. Formation from the bromide is however relatively rapid, reaction times of e.g. 12 hours being frequently sufiicient dependent on the reaction temperature employed.

The 21-hydrocarbonsulphonyloxy compounds can be prepared from the corresponding 21-hydroxy compounds in conventional manner e.g. by reaction with a hydrocarbon sulphonyl halide in the presence of a tertiary base e.g. pyridine.

The processes according to the invention are particularly useful for the production of various 17a-monoesters of 21-deoxybetamethasone and 2l-deoxydexamethasone, e.g. compounds having the formula:

o ---ooon IIO (where R is a a straight or branched chain alkyl group having from 1 to 9 carbon atoms in particular an alkyl group containing a straight chain of up to three carbon atoms which may be branched with a methyl group) and especially the compounds of our copending application S.N. 466,434, filed June 23, 1965, now Pat. No. 3,376,- 193.

The processes according to the invention are also useful in the production of A pregnane compounds particularly those used as starting materials for the preparation of topically active steroids according to our copending application S.N. 559,067, filed June 21, 1966, now abandoned. These starting materials may thus be prepared by converting a 17u,21-diol to the corresponding 21-ol-17a-acyloxy compound via a 17a,21-orthoester, converting to a 21-hydrocarbonsulphonyloxy compound of Formula I and then proceeding according to a process of the present invention. The A starting materials are also useful for conversion to the compounds of IV where R has the meaning given above.

The invention will now be illustrated with reference to the following examples in which all temperatures are in degrees Centigrade.

EXAMPLE 1 (a) 9a-flllO1'O-1 lfl-hydroxy-Zl-methanesulphonyloxy-16p3- methyl-17a-propionyloxypregna-1,4-diene-3,20-dione 9a fiuoro 1113,21 dihydroxy 16B methyl 17ozpropionyloxypregna-1,4-diene-3,20-dione (5.3 g.) in pyridine (20 ml.) was treated with methanesulphonyl chloride (5 ml.) and the mixture was left at room temperature'for min. It was then poured into ice-cold N-hydrochloric acid with shirring. The 2l-methanesulphonate was filtered off and crystallised from aqueous ethanol, to give 4.5 g. of material, M.P. 177-179, [d] +80 (c. 0.5 in CHCl A max. (in EtOH)238-240 my (e 14,800) (found: C, 58.2; H, 7.0. C H FO S. /2H O requires C, 58.2; H, 6.8%).

(b) 9a-fluoro-1 1 fl-hydroxy-l 6fl-methyl- 17 a-propionyloxypregna-1,4-diene-3,20-dione 9u-fluoro-1lfl-hydroxy-Zl-methanesulphonyloxy 16B- methyl 17cc propionyloxypregna-l,4-diene-3,20-dione (1 g.) in pyridine (50 ml.) was treated with soduim iodide (3 g.) and the mixture was heated at for 6 hrs. It was then poured into dilute hydrochloric acid and extracted with chloroform. The extract was washed successively with aqueous sodium bicarbonate, aqueous sodium thiosulphate and water, dried (MgSO and evaporated to dryness. The residue was chromatographed on neutral alumina (Grade III; 50 g.); the material eluted by etherbenzene (1:3) was crystallised from acetone-hexane to give 9a-fiuoro-1lfl-hydroxy-l6,3-methyl-17a-propionyloxypregna 1,4 diene 3,20 vdione (270 mg.) M.P. 238- 241, [eth l-75 (c. 1.0 in CHCl EXAMPLE 2 (a) 9a-fluoro-11/3-hydr0xy-2l-methanesulphonyloxy-l6,8- methyl-l7a-valeryloxypregna-1,4-diene-3,20-dione A solution of 9u-fluor0-1113,2l-dihydroxy-16 3-methyll7a-valer-yloxypregna-1,4-diene-3,20-dione (2 g.) in pyridine (17.2 ml.) was cooled to 0 and treated with methanesulphonyl chloride (1.72 ml.). After standing for 15 min. at 0 the mixture was poured into iced 0.5 N hydrochloric acid,. and the precipitate was collected, and washed with sodium bicarbonate and water. The material was dried in vacuo over potassium hydroxide at room temperature to give the methane-sulphonate (2.25 g.) as an amorphous solid, M.P. ca. 76 dec. [a] |71.0 (c. 1.3 in dioxan), A max. (in EtOI-I) 239 my. (6 15,580) (found: C, 60.45; H, 7.4; S, 5.8. C H FO S requires C, 60.6; H, 7.1; S, 5.8%).

(b) 21-brom0-9a-fiuoro-11fi-hydroxy-16fl-methyl-l7avaleryloxypregna-1,4-diene-3 ,20-dione A solution of 9a-fluoro-llfi-hydroxy-Zl-methanesulphonyloxy-l6 8-methyl-l7a valeryloxypregna-1,4-diene- 3,20-dione (4 g.) in acetone (200 ml.) was treated with anhydrous lithium bromide (12 g.) and the mixture was refluxed for 3 days. The acetone was removed in vacuo and the residue partitioned between chloroform and water. The chloroform fraction, after evaporation and crystallisation from ether, gave the 21-bromo compound (3.0 g.) as prisms, M.P. 148-149" C. (dec.), [u] +99.3 (c. 1.6 in dioxan), )t max. (in EtOH) 238-239 m (6 16,620) (found: C, 60.5; H, 6.9; Br, 14.6. C I-I BrFO requires C, 60.1; H, 6.7; Br, 14.8%).

( c) 9a-fluoro-1 lfi-hydroxy-Z1-iodo-16fi-methy1-17avaleryloxypregna-1,4-diene-3 ,20-dione (i) A solution of 2l-bromo-9a-fluoro-lIB-hydroxy- 16B methyl-17a-valeryloxypregna-1,4-diene-3,20-dione (1.66 g.) in acetone (75 ml.) was treated with sodium iodide (3.3 g.) and the mixture refluxed overnight. The acetone was removed in vacuo and the residue partitioned between ether and water. The ether fraction, by evaporation and crystallisation of the residue from aqueous acetone, gave the 21-iodo compound (1.53 g.) as fine needles, M.P. 129-130" (dec.), [a] |106.2 (c. 1.4 in dioxan), A max. (in EtOH) 237-239 ma (6 16,480) (found: C, 55.8; H, 6.45; I, 21.1. C H FIO requires C, 55.3; H, 6.2; I, 21.6%).

(ii) A solution of 9u-fluoro-1lfi-hydroxy-Zl-methanesulphonyl0xy-16 3-methyl 17oz valeryloxypregna-1,4- diene-3,20-dione (200 mg.) in acetone (5 ml.) was treated with sodium iodide (400 mg.) and the mixture refluxed on a steam bath. After 8 days, ca. 75% con version to 2l-iodo-compound had occurred, as judged by spot intensities on thin-layer chromatography.

(d) 9a-fluoro-11B-hydroxy-16B-methyl-17a-valery1oxypregna-1,4-diene-3,20-dione A solution of 9a-fluoro-1 lfl-hydroxy-Zl-iodo-16fl-methyl-l7u-valeryloxyphegna-1,4-diene-3,20-dione (50 mg.) in pyridine (1.25 ml.) was heated on the steam bath for 3 /2 hours. The mixture was poured into water and extracted with chloroform and the isolated material (40 mg.) chromatographed on Grade IV neutral alumina to give, on elution with ether and crystallisation from benzene-petroleum, 9a-flu010 11/3-hydroxy-165-methyl-17a-valeryloxypregna-1,4-diene-3,20-dione mg.).

EXAMPLE 3 9a-fluoro-1 lfi-hydroxy-l 6fi-methyl-17a-valeryloxypregna- 1,4-diene-3 ,20-dione A solution of 9a-fluoro-1lfi-hydroxy-Zl-methanesulphonyloxy-16B-methyl-17u valeryloxypregna-1,4-diene- 3,20-dione (500 mg.) in pyridine (12.5 ml.) was treated with sodium iodide (1 g.) and the mixture was heated on the steam bath for 6 hrs. The mixture was poured into water and the solid (383 mg.) isolated by filtration. Chloroform extraction of the filtrate afforded a further crop (30 mg.) of product. The combined solids, in acetone, were filtered through Florisil (magnesium trisilicate) to remove some of the colour and the residue, in benzene, was chromatographed on Grade IV neutral alumina (5.5 g.). Elution was ether and crystallisation of the fractions (twice) from benzene-petroleum gave 9zx-fill01'0- 11B hydroxy 161? methyl l7u-valeryloxypregna-1,4- diene-3,20-dione (171 mg.) as fine needles, M.P. 195- 196, [a] +64.9 (c. 1.3 in CHCl Its infrared spectrum was identical with that of an authentic sample.

EXAMPLE 4 9a fluoro-1lfi-hydroxy-16fi-methyl-17u-valeryloxypregna- 1,4-diene 3,20 dione from 9a-fll10l0-11B-I1YdI'OXY-21- iodo-l6B-methyl-17u-valeryloxypregna-1,4-diene 3,20- dione (a) With pyridine-A solution of 9u-fluoro-11B-hydroxy 21 iodo-16fl-methyl-17a-valeryloxypregna-1,4- diene-3,20-dione (50 mg.) in pyridine (2 ml.) was heated on the steam bath for 3 hours. The mixture was evaporated to dryness, dissolved in chloroform and put on a small column of Grade IV neutral alumina. The column was eluted with ether and the material obtained was crystallised from chloroform-petroleum to give 9oc-fiu0rO-11B- hydroxy-16,8-methyl 17a valeryloxypregna-1,4-diene- 3,20-dione (27 mg., 69% yield) with infrared spectrum identical to that of an authentic sample.

(b) With triethylamine.A solution of the 21-iodo compound (50 mg.) in triethylamine (2 ml.) was heated on the steam bath for 5 hours and then worked up as in Example 4(a). crystallisation from chloroform-petroleum gave 9a-fluoro-11fi-hydroxy 16B methyl-17avaleryloxypregna-1,4-diene-3,20-dione (32.7 mg., 83.5% yield) with an infrared spectrum identical to that of an authentic sample.

(c) With dimethyl sulphoxide.A solution of the 21- iodo compound (50 mg.) in dimethylsulphoxide (2 ml.) was heated on the steam bath for 20 hours and worked up in the usual way to give an oily solid. This material was purified by preparative thin layer chromatography to give unchanged 21-iodo compound 5 mg.) and 9a fluoro-llfi-hydroxy 165 methyl-17a-valeryloxypregna-1,4-diene-3,20-dione (24.5 mg, 62.5% yield).

EXAMPLE 5 9a fluoro 116 hydroxy 165 methyl-17u-valeryloxypregna-1,4-diene-3,20-dione from 21-bromo-9a-fluoro- 1 11/3 hydroxy 16,6 methyl-17a-valeryloxypregna-1,4-

diene-3,20-dione (a) With sodium iodide in pyridine-A solution of 21- bromo 9oz fluoro-11,8-hydroxy-16fl-methyl-17a-valeryl oxypregna-1,4-diene-3,20-dione (50 mg.) and sodium iodide (100 mg.) in pyridine (2 ml.) was heated on the steam bath for 3 hours. The pyridine was removed in vacuo and the residue, in chloroform, filtered through a small plug of Grade IV neutral alumina. The plug was washed with ether, the washings combined and evaporated 6 to give 9a-fluoro-1 l ,B-hydroxy-16,8-methyl-17u-valeryloxypregna-1,4-diene-3,20-dione (30 mg, 70%) with infrared spectrum identical to that of an authentic sample.

(b) With sodium iodide in triethylamine-A suspension of 21-bromo-9a-fiuoro-1lfl-hydroxy-16fi-methyl-17avaleryloxypregna-1,4-diene-3,20-dione (50 mg.) and sodium iodide mg.) in triethylamine (2 ml.) was heated on the steam bath for 8 hours, The solvent was removed in vacuo and the residue treated as above to give 9u-fluorohydroxy 16,8 methyl 17a-valeryloxypregna-1,4 diene-3,20-dione (39.6 mg, 93%

(0) With sodium iodide in triethylamine-acetone.-A solution of 21-bromo-9a-fluoro-1lfi-hydroxy-lGfi-methyl- 17a-valeryloxypregna-1,4-diene-3,20-dione (50 mg.) and sodium iodide (100 mg.) in acetone (1.5 ml.) and triethylamine (1.5 ml.) was heated on the steam bath for 18 hours. Working up as described above gave 9a-fiuoro- 11B hydroxy methyl 17a-valeryloxypregna-1,4- diene-3,20-dione (39.6 mg., 93%

EXAMPLE 6 (a) 16(3-methyl- 1741,21 1-ethyll -ethoxymethylenedioxy)pregna-1,4,9-triene-3 ,20-dione A solution of 17a,21 dihydroxy 16B methylpregna- 1,4,9-triene-3,20-dione (500 mg.) in dioxan (20 ml.) was treated with triethyl ortho-propionate (0.7 ml.) and ptoluenesulphonic acid (ca. 5 mg). After standing at room temperature for 40 minutes the mixture was poured into dilute sodium bicarbonate and the product isolated by filtration. crystallisation from ether gave 16 8-methyl 17a,21(1'-ethyl 1' ethoxymethylenedioxy)pregna-1,4,9 triene-3,20-dione (340 mg.) as cubic prisms M.P 177 C., [a] +5.2 (c. 1.0 dioxan), max. (in EtOH) 238-239 mg (e 16,000). (Found: C, 73.4; H, 8.5. C H O requires C, 73.6; H, 8.25%.)

(b) 21-hydroxy-16,3-methyl-17a-propionyloxypregna-1,4,9-triene3 ,20-dione Uncrystallised 16B methyl 17a,21(1'-ethyl-1'-ethoxymethylenedioxy)pregna- 1,4,9-triene-3,20-dione obtained from 17a,21-hydroxy-16fi-methylpregna-1,4,9-triene-3,20 dione (8.0 g.) as described in Example 6(a) was dissolved in acetic acid (95 ml.) containing water (8 ml.) and kept at room temperature for 40 minutes. Dilution with water and filtration gave the crude product. Crystallisation of this material from other (containing a little acetone)-petroleum gave 21-hydroxy 16B methyl-17apropionyloxypregna-1,4,9-triene-3,20-dione (7.52 g.) as large prismS, M.P. 177-179 C., [u] +16.1 (c. 0.9 dioxan), 7x max. (in EtOH) 237238 m (6 16,210). (Found: C, 73.0; H, 7.9. C H O requires C, 72.8; H, 7.8%.)

(c) 16fl-methyl-17a-propionyloxypregna- 1,4,9-triene-3 ,20-dione A solution of 2l-hydroxy-16/3-methy1-17a-propionyloxypregna-1,4,9-triene-3,20-dione (6.7 g.) in dry pyridine (50 ml.) was treated, at 0, with methanesulphonyl chloride (1.87 ml.). After standing at room temperature for 1 hour the mixture was poured with stirring into iced N-hydrochloric acid. Filtration gave the ZI-methanesulphonate (7.9 g., 99%) as a white amorphous solid.

The methanesulphonate (7 g.) in pyridine (200 ml.) was treated with sodium iodide (14 g.) and the mixture was heated on the steam bath for 5 hours. The pyridine was removed in vacuo and the dark oily residue was dissolved in chloroform and filtered through silica gel. The silica gel was washed with ether and the washings evaporated to give a pale yellow crystalline solid. Crystallisation of this material from ether, then from ether-petroleum, gave 16fi-methyl-17a-propionyloxypregna-1,4,9-triene-3,20-dione (2.88 g.) as silky needles, M.P. 177- 179 C., [a] +2.7 (c. 1.1 dioxan), A max. (in EtOH) 237-238 my. (6 15,580). (Found: C, 75.75; H, 8.1. C H O requires C, 75.7; H, 8.15%.)

7 EXAMPLE 7 (a) 9a-fiuoro 118,21 dihydroxy-l6a-methyl-l7-propionyloxypregna-l,4-diene-3,20-dione (dexamethasone l7- propionate) Dexamethasone g.) was dissolved in dioxan (200 ml.) and p-toluenesulphonic acid (400 mg.) and triethyl orthopropionate ml.) were added. The solution was allowed to stand at room temperature for 1 hr. and was then poured into sodium bicarbonate solution. The white solid was filtered off and dried at 100 C. to give dexamethasone 17,21-ethyl orthopropionate (5.83 g.).

This material was dissolved in acetone (240 ml.) and water (48 ml.) and 2 N sulphuric acid (2.4 ml.) were addedrThe solution was allowed to stand at room temperature for 30 min. and was then poured into water; the product was isolated with chloroform. The crude solid was crystallised from acetone-hexane to give 9a-fill0l'0- 11fl,21-dihydroxy 16oz methyl-l7-propionyloxypregna- 1,4-diene-3,20-dione (3.6 g.), M.P. 219223 C., [ab-6 (c, 1.0 in CHCl 1 238 m (E cm. 351). (Found: C, 67.25; H, 7.0. C H FO requires C, 67.0; H, 7.4%.)

(b) 9a-fiIl0IO-l lfl-hydroxy 21 methanesulphonyloxy- 16oz methyl 17 propionyloxypregna 1,4 diene- 3,20-dione Dexamethasone 17-propionate (3 g.) was dissolved in pyridine ml.) and the solution was cooled to 10 C. Methanesulphonyl chloride (3 ml.) was added and the temperature was kept at about 20 for 30 minutes. The reaction mixture was poured into cold dilute 2 N hydrochloric acid and the white solid was filtered off and dried (3.3 g.). It was then crystallised from acetone-hexane to give the methanesulphonate (2.9 g); M.P. 183- 186 C. (decomp.); [eth l-46 (c. 1.0 in CHCl kmax, 238 rn (E cm. 308). (Found: C, 59.6; H, 6.5; S, 6.1. C H FO S requires C, 59.3; H, 6.7; S, 6.1%.)

(c) 90: fluoro 1113 hydroxy 16a methyl l7 propionyloxypregna 1,4 diene 3,20 dione (2l-deoxydexamethasone 17-propionate) 9a fluoro 11,8 hydroxy 21 methanesulphonyloxy- 16a-methyl-l7-propionyloxypregna-l,4-diene-3,20 dione (500 mg.) was dissolved in pyridine (25 ml.) and sodium iodide (2.5 g.) was added. The solution was heated in an oil bath maintained at 105 C. for 17 hrs. and was then cooled and poured into cold 2 N hydrochloric acid and extracted with chloroform. The extract was washed with water, sodium thiosulphate solution and water and was dried (MgSO The solution was then evaporated and the residue was crystallised from acetone-hexane to give 2l-deoxydexamethasone 17-propionate (140 mg); M.P. 216219; [a] +50 (c. 1 in CHCI k 239 m (E cm. 367). (Found: C, 69.4, H, 7.5. C H 'FO requires C, 69.3; H, 7.7%.)

I claim:

1. A process for the preparation of a 2l-unsubstitutedl7a-acyloxy steroid of the pregnane series having at position 17 the formula:

)YOCOR "OCOR 17 wherein X is a member of the group consisting of bromine, hydrocarbonsulfonyloxy and iodine-and R, in each instance, is an alkyl, cycloalkyl, cycloalkylalkyl or aralkyl group, with a member of the group consisting of a tertiary amine and a dialkylsulfoxide and, when X is bromine and hydrocarbonsulfonyloxy, in the presence of a metal iodide.

2. A process as claimed in claim 1 wherein the 21- substituted steroid is heated with pyridine.

3. A process as claimed in claim 1 wherein the 21- substituted steroid is heated with a trialkylamine.

4. A process as claimed in claim 3 wherein the trialkylamine is triethylamine.

5. A process as claimed in claim 1 wherein the 21- substituted steroid is heated with dimethylsulfoxide.

6. A process as claimed in claim 1 wherein the 21- substituted steroid is heated in the presence of an inert solvent selected from the group consisting of acetone, methylethyl ketone, methanol, ethanol, isopropanol and dimethylformamide.

7. A process as claimed in claim 1 wherein the reaction is conducted at a temperature of from 60 C. to C.

8. A process as claimed in claim 1 wherein the metal iodide is a member of the group consisting of alkali metal iodides and alkaline earth metal iodides.

9. A process as claimed in claim 1 wherein X is a hydrocarbon sulfonyloxy group which contains an alkyl group having from 1 to 6 carbon atoms.

10. A process as claimed in claim 9 wherein X is a hydrocarbon sulfonyloxy group which contains a phenyl group.

11. A process as claimed in claim 1 wherein a starting steroid in which X is iodine is heated with a member of the group consisting of pyridine, triethylamine and dimethylsulfoxide at a temperature from 60 C. to 120 C.

12. A process as claimed in claim 1 wherein a starting steroid in which X is bromine is heated with a member of the group consisting of pyridine, triethylamine and dimethylsulfoxide at a temperature from 60 C. to 120 C.

13. A process as claimed in claim 12 wherein the metal iodide is a member of the group consisting of alkalimetal iodides and alkaline earth metal iodides.

14. A process as claimed in claim 1 wherein a starting steroid in which X is hydrocarbonsulfonyloxy is heated with a member of the group consisting of pyridine, triethylamine and dimethylsulfoxide at a temperature from 60 C. to 120 C.

15. A process as claimed in claim 14 wherein the metal iodide is a member of the group consisting of alkalimetal iodides and alkaline earth metal iodides.

16. A process as claimed in claim 11 wherein the starting steroid is a 17-acyloxy ester of 9ot-fillOIO-llfl,l7adihydroXy-16-methyl-2l-iodo-pregna 1,4 diene 3,20- dione.

17. A process as claimed in claim 12 wherein the starting steroid is a 17-acyloxy ester of 9a-flL1OIO-llB,l7a-dihydroxy 16 methyl 21 bromo pregna 1,4 diene- 3,20-dione.

18. A process as claimed in claim 14 wherein the starting steroid is a 17-acyloxy ester of 9a-fluoro-1lB,17a-dihydroxy 16 methyl 21 hydrocarbonsulfonyloxypregna-1,4-diene-3,20-dione.

References Cited UNITED STATES PATENTS ELBERT L. ROBERTS, Primary Examiner.

U.S. Cl. X.R. 

